Date published: 2026-2-22

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IRP-1 Activators

The class of IRP-1 activators comprises a diverse array of chemicals that modulate cellular processes involved in iron metabolism. These compounds offer unique avenues for exploring the activation or modulation of IRP-1 and its regulatory functions. Nitric oxide, a signaling molecule, indirectly activates IRP-1 by influencing cellular redox status, providing insights into the redox-sensitive regulatory mechanisms of IRP-1. L-ascorbic acid (Vitamin C) enhances non-heme iron absorption, indirectly influencing IRP-1 activity and its regulation of iron-responsive elements (IREs).

Metabolites such as alpha-ketoglutarate, succinic acid, and cis-aconitic acid, from cellular energy metabolism, indirectly activate IRP-1 by impacting cellular energy status. These chemicals highlight the intricate connection between cellular energy metabolism and iron homeostasis, suggesting avenues for exploration. Electrophiles like diethyl maleate and dimethyl fumarate induce oxidative stress, providing a unique approach to indirectly activate IRP-1 through modulation of cellular redox conditions. Compounds such as succinylacetone and sodium nitroprusside act through diverse mechanisms, influencing heme biosynthesis and releasing nitric oxide, respectively, to impact IRP-1 activity. These chemicals open avenues for understanding the complex regulatory networks governing IRP-1 function. The class of IRP-1 activators offers valuable tools for investigating the dynamic interplay between cellular processes, energy metabolism, and iron homeostasis, contributing to a deeper understanding of IRP-1-mediated pathways in health and disease.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

L-Ascorbic acid, free acid

50-81-7sc-202686
100 g
$46.00
5
(1)

L-ascorbic acid, commonly known as Vitamin C, acts as an indirect activator of IRP-1 by influencing iron availability. Vitamin C enhances non-heme iron absorption, potentially impacting the activity of IRP-1 and its regulation of iron-responsive elements (IREs). This chemical modulation of iron homeostasis through Vitamin C administration provides a potential avenue for indirectly influencing IRP-1-mediated processes involved in iron metabolism.

α-Ketoglutaric Acid

328-50-7sc-208504
sc-208504A
sc-208504B
sc-208504C
sc-208504D
sc-208504E
sc-208504F
25 g
100 g
250 g
500 g
1 kg
5 kg
16 kg
$33.00
$43.00
$63.00
$110.00
$188.00
$738.00
$2091.00
2
(1)

Alpha-ketoglutarate, an intermediate in the Krebs cycle, acts as an indirect activator of IRP-1 by influencing cellular energy metabolism. The Krebs cycle-derived metabolite may impact the activity of IRP-1, as cellular energy status is known to influence iron homeostasis.

Succinic acid

110-15-6sc-212961B
sc-212961
sc-212961A
25 g
500 g
1 kg
$45.00
$75.00
$133.00
(0)

Succinic acid, a key intermediate in cellular metabolism, acts as an indirect activator of IRP-1 by influencing cellular energy status. The metabolite may impact the activity of IRP-1, as cellular energy levels are known to influence iron homeostasis.

cis-Aconitic acid

585-84-2sc-257251
sc-257251A
1 g
5 g
$99.00
$405.00
(0)

Cis-aconitic acid, an isomer of aconitic acid in the Krebs cycle, acts as an indirect activator of IRP-1 by influencing cellular energy metabolism. The metabolite may impact the activity of IRP-1, as cellular energy status is known to influence iron homeostasis.

Diethylmaleate

141-05-9sc-202577
5 g
$27.00
4
(1)

Diethylmaleate acts as an indirect activator of IRP-1 by influencing cellular redox status. As an electrophile, diethyl maleate can induce oxidative stress, potentially impacting the redox-sensitive regulatory function of IRP-1. The exact mechanism through which diethyl maleate affects IRP-1 requires further investigation, but this chemical provides a unique avenue for exploring the modulation of IRP-1-mediated processes through alterations in cellular redox conditions.

Succinylacetone

51568-18-4sc-212963
sc-212963B
10 mg
100 mg
$336.00
$418.00
(1)

Succinylacetone, an inhibitor of delta-aminolevulinic acid dehydratase (ALAD), indirectly activates IRP-1 by influencing heme biosynthesis. By inhibiting ALAD, succinylacetone disrupts heme synthesis, potentially impacting the activity of IRP-1 and its regulation of iron-responsive elements (IREs).

Dimethyl fumarate

624-49-7sc-239774
25 g
$28.00
6
(1)

Dimethyl fumarate acts as an indirect activator of IRP-1 by influencing cellular redox status. As an electrophile, dimethyl fumarate induces oxidative stress, potentially impacting the redox-sensitive regulatory function of IRP-1. The exact mechanism through which dimethyl fumarate affects IRP-1 requires further investigation, but this chemical provides a unique avenue for exploring the modulation of IRP-1-mediated processes through alterations in cellular redox conditions.

α-Lipoic Acid

1077-28-7sc-202032
sc-202032A
sc-202032B
sc-202032C
sc-202032D
5 g
10 g
250 g
500 g
1 kg
$69.00
$122.00
$212.00
$380.00
$716.00
3
(1)

Alpha-lipoic acid acts as an indirect activator of IRP-1 by influencing cellular redox status. As a potent antioxidant, alpha-lipoic acid modulates oxidative stress, potentially impacting the redox-sensitive regulatory function of IRP-1. The exact mechanism through which alpha-lipoic acid affects IRP-1 requires further investigation, but this chemical provides a unique avenue for exploring the modulation of IRP-1-mediated processes through alterations in cellular redox conditions.

L-Methionine

63-68-3sc-394076
sc-394076A
sc-394076B
sc-394076C
sc-394076D
sc-394076E
25 g
100 g
250 g
1 kg
5 kg
10 kg
$34.00
$37.00
$57.00
$151.00
$577.00
$1103.00
(0)

L-methionine, an essential amino acid, acts as an indirect activator of IRP-1 by influencing cellular redox status. As a precursor to glutathione, L-methionine can modulate oxidative stress, impacting the redox-sensitive regulatory function of IRP-1.

Sodium nitroprusside dihydrate

13755-38-9sc-203395
sc-203395A
sc-203395B
1 g
5 g
100 g
$43.00
$85.00
$158.00
7
(1)

Sodium nitroferricyanide(III) dihydrate acts as an indirect activator of IRP-1 by releasing nitric oxide (NO), influencing cellular redox status. NO modulates oxidative stress, impacting the redox-sensitive regulatory function of IRP-1. The exact mechanism through which sodium nitroprusside affects IRP-1 requires further investigation, but this chemical provides a unique avenue for exploring the modulation of IRP-1-mediated processes through alterations in cellular redox conditions.